OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C
K-Number: K881601 · 1988-06-15
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Device Summary
Frequently Asked Questions
What is the OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C?
OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C is a medical device that received FDA 510(k) clearance on 1988-06-15. The listed applicant is Omron Tateisi Electronics Co.. The 510(k) number is K881601.
When did OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C receive FDA 510(k) clearance?
OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C received FDA 510(k) clearance on 1988-06-15, under 510(k) number K881601.
Who is the listed applicant for OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C?
The FDA 510(k) record lists Omron Tateisi Electronics Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C?
The FDA product code for OMRON DIGITAL BLOOD PRESSURE MONITOR MODEL HEM403C is DXN.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing Omron Tateisi Electronics Co. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DXN)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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